TNF-α tolerance blocks LPS-induced hypophagia but LPS tolerance fails to prevent TNF-α-induced hypophagia

被引:37
作者
Porter, MH [1 ]
Arnold, M [1 ]
Langhans, W [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Anim Sci Physiol & Anim Husb, CH-8092 Zurich, Switzerland
关键词
tumor necrosis factor-alpha; lipopolysaccharide; anorexia; cytokine; endotoxin; food intake; feeding;
D O I
10.1152/ajpregu.1998.274.3.R741
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
To investigate the role of tumor necrosis factor-alpha (TNF-alpha) in bacterial lipopolysaccharide (LPS)-induced hypophagia, we tested whether a cross tolerance between LPS and TNF-alpha exists with respect to their anorectic effects. Only the first of three subsequent intraperitoneal injections of LPS (100 mu g/kg body wt) given every second day at dark onset (12:12-h light-dark cycle) led to a significant reduction of food intake in male rats. Likewise, intraperitoneal injections of human recombinant TNF-alpha (150 mu g greater than or equal to 3 x 10(6) U/kg body wt) also resulted in tolerance to its hypophagic effect. LPS tolerance did not alter the hypophagic response to subsequently injected TNF-alpha (n = 14). However, TNF-alpha pretreatment completely blocked the hypophagic response to LPS (n = 14). The results demonstrate that tolerance to the hypophagic effect of exogenous TNF-alpha is sufficient to eliminate LPS-induced hypophagia. This is consistent with the hypothesis that endogenous TNF-alpha plays a major role in LPS-induced hypophagia. The ineffectiveness of LPS tolerance to attenuate TNF-alpha-induced hypophagia is compatible with findings demonstrating that reduced TNF-alpha production is an important feature of LPS tolerance.
引用
收藏
页码:R741 / R745
页数:5
相关论文
共 34 条
[1]   Endotoxin tolerance impairs a pertussis-toxin-sensitive G-protein regulating tumour necrosis factor release by macrophages from tumour-bearing rats [J].
Altavilla, D ;
Squadrito, F ;
Canale, P ;
Ioculano, M ;
Campo, GM ;
Squadrito, G ;
Urna, G .
PHARMACOLOGICAL RESEARCH, 1996, 33 (03) :203-209
[3]   IDENTITY OF TUMOR NECROSIS FACTOR AND THE MACROPHAGE-SECRETED FACTOR CACHECTIN [J].
BEUTLER, B ;
GREENWALD, D ;
HULMES, JD ;
CHANG, M ;
PAN, YCE ;
MATHISON, J ;
ULEVITCH, R ;
CERAMI, A .
NATURE, 1985, 316 (6028) :552-554
[4]  
COOK JA, 1985, HDB ENDOTOXIN CELLUL, P303
[5]   Biologic basis for interleukin-1 in disease [J].
Dinarello, CA .
BLOOD, 1996, 87 (06) :2095-2147
[6]   DIFFERENTIAL REGULATION OF CYTOKINE PRODUCTION IN LIPOPOLYSACCHARIDE TOLERANCE IN MICE [J].
ERROI, A ;
FANTUZZI, G ;
MENGOZZI, M ;
SIRONI, M ;
ORENCOLE, SF ;
CLARK, BD ;
DINARELLO, CA ;
ISETTA, A ;
GNOCCHI, P ;
GIOVARELLI, M ;
GHEZZI, P .
INFECTION AND IMMUNITY, 1993, 61 (10) :4356-4359
[7]   TOLERANCE TO TUMOR NECROSIS FACTOR IN RATS AND THE RELATIONSHIP TO ENDOTOXIN TOLERANCE AND TOXICITY [J].
FRAKER, DL ;
STOVROFF, MC ;
MERINO, MJ ;
NORTON, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (01) :95-105
[8]  
FRANKENBERGER M, 1995, J INFLAMM, V45, P56
[9]  
GOLDBACH JG, 1996, AM J PHYSIOL, V270, pRM49
[10]   MECHANISMS OF ENDOTOXIN TOLERANCE .4. SPECIFICITY OF PYROGENIC REFRACTORY STATE DURING CONTINUOUS INTRAVENOUS INFUSIONS OF ENDOTOXIN [J].
GREISMAN, SE ;
YOUNG, EJ ;
WOODWARD, WE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1966, 124 (05) :983-&